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441074

Sigma-Aldrich

2-Bromo-4,5-dimethoxybenzoic acid

98%

Synonym(s):

6-Bromoveratric acid

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About This Item

Linear Formula:
BrC6H2(OCH3)2CO2H
CAS Number:
Molecular Weight:
261.07
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

mp

188-190 °C (lit.)

SMILES string

COc1cc(Br)c(cc1OC)C(O)=O

InChI

1S/C9H9BrO4/c1-13-7-3-5(9(11)12)6(10)4-8(7)14-2/h3-4H,1-2H3,(H,11,12)

InChI key

HWFCHCRFQWEFMU-UHFFFAOYSA-N

Related Categories

General description

2-Bromo-4,5-dimethoxybenzoic acid is a 2-halo-4,5-dialkoxybenzoic acid derivative.

Application

2-Bromo-4,5-dimethoxybenzoic acid may be used as starting material for the synthesis of norathyriol and urolithins.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

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Hideyuki Ito et al.
Journal of agricultural and food chemistry, 56(2), 393-400 (2008-01-01)
Hydrolyzable tannins, including ellagitannins, occur in foods such as berries and nuts. Various biological activities, including antioxidant, antiviral, and antitumor activities, have been noted and reported for ellagitannins, but the absorption and metabolism of purified ellagitannins are poorly understood. We
Peter Lorenz et al.
Chemistry & biodiversity, 15(5), e1800035-e1800035 (2018-03-27)
Seeds from Hypericum species have recently been identified as an interesting source of xanthone derivatives. Extraction of seeds from H. perforatum with MeOH and subsequent concentration via polyamide adsorption yielded a fraction enriched in tetrahydroxyxanthones (THX), which were further semipurified
A facile synthesis of norathyriol.
Qin Q-X, et al.
J. Chem. Res. (M), 37(1), 38-39 (2013)
Sashi G Kasimsetty et al.
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The cytochrome P450 enzyme, CYP1B1, is an established target in prostate cancer chemoprevention. Compounds inhibiting CYP1B1 activity are contemplated to exert beneficial effects at three stages of prostate cancer development, that is, initiation, progression, and development of drug resistance. Pomegranate

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